17515-18-3Relevant articles and documents
Asymmetric syntheses of (-)-methyl shikimate and (-)-5a-carba-β-d-gulopyranose from d-arabinose via Mukaiyama-type intramolecular aldolization
Liu, Shi-Ling,Shi, Xiao-Xin,Xu, Yu-Lan,Xu, Wei,Dong, Jing
experimental part, p. 78 - 83 (2009/06/06)
New asymmetric syntheses of (-)-methyl shikimate 1 and (-)-5a-carba-β-d-gulopyranose 11 from d-arabinose through a common route which employed Mukaiyama-type intramolecular aldolization as a key step were described.
Synthese de derives des acides quinique et shikimique
Delfourne, Evelyne,Despeyroux, Pierre,Gorrichon, Liliane,Veronique, Jacqueline
, p. 532 - 544 (2007/10/02)
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A NEW SYNTHETIC ROUTE TO METHYL (-)-SHIKIMATE BY ASYMMETRIC DIELS-ALDER REACTON OF (S)S-3-(2-PYRIDYLSULFINYL)ACRYLATE
Takahashi, Tamiko,Namiki, Toshie,Takeuchi, Yoshio,Koizumi, Toru
, p. 3213 - 3215 (2007/10/02)
A 7-oxabicycloheptene derivative (7a) that substituted effectively for the synthesis of (-)-shikimic acid was prepared by an asymmetric Diels-Alder reaction of (S)s-3-(2-pyridylsulfinyl)acrylate (2) with 3,4-dibenzyloxyfuran (4).The bicy